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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder)
... > Clinical finding (finding) > disease > Disorder of body system > Visual system disorder > Disorder of vision > Visual impairment (disorder) > Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder)
... > Clinical finding (finding) > Eye finding > Visual system disorder > Disorder of vision > Visual impairment (disorder) > Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder)
Hereditary cerebellar degeneration > Hereditary cerebellar atrophy (disorder) > Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder)

Preferred term

Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder)  

Type

  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

Associated morphology

Clinical course

URI

http://www.irandoc.acir/onto/irandoc/1172696009

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